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Model-based design for seizure control by stimulation
OBJECTIVE. Current brain stimulation paradigms are largely empirical rather than theoretical. An opportunity exists to improve upon their modest effectiveness in closed-loop control strategies with the development of theoretically grounded, model-based designs. APPROACH. Inspired by this need, here...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8341467/ https://www.ncbi.nlm.nih.gov/pubmed/32103826 http://dx.doi.org/10.1088/1741-2552/ab7a4e |
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author | Ashourvan, Arian Pequito, Sérgio Khambhati, Ankit N Mikhail, Fadi Baldassano, Steven N Davis, Kathryn A Lucas, Timothy H Vettel, Jean M Litt, Brian Pappas, George J Bassett, Danielle S |
author_facet | Ashourvan, Arian Pequito, Sérgio Khambhati, Ankit N Mikhail, Fadi Baldassano, Steven N Davis, Kathryn A Lucas, Timothy H Vettel, Jean M Litt, Brian Pappas, George J Bassett, Danielle S |
author_sort | Ashourvan, Arian |
collection | PubMed |
description | OBJECTIVE. Current brain stimulation paradigms are largely empirical rather than theoretical. An opportunity exists to improve upon their modest effectiveness in closed-loop control strategies with the development of theoretically grounded, model-based designs. APPROACH. Inspired by this need, here we couple experimental data and mathematical modeling with a control-theoretic strategy for seizure termination. We begin by exercising a dynamical systems approach to model seizures (n = 94) recorded using intracranial EEG (iEEG) from 21 patients with medication-resistant, localization-related epilepsy. MAIN RESULTS. Although each patient’s seizures displayed unique spatial and temporal patterns, their evolution can be parsimoniously characterized by the same model form. Idiosyncracies of the model can inform individualized intervention strategies, specifically in iEEG samples with well-localized seizure onset zones. Temporal fluctuations in the spatial profiles of the oscillatory modes show that seizure onset marks a transition into a regime in which the underlying system supports prolonged rhythmic and focal activity. Based on these observations, we propose a control-theoretic strategy that aims to stabilize ictal activity using static output feedback for linear time-invariant switching systems. Finally, we demonstrate in silico that our proposed strategy allows us to dampen the emerging focal oscillatory sources using only a small set of electrodes. SIGNIFICANCE. Our integrative study informs the development of modulation and control algorithms for neurostimulation that could improve the effectiveness of implantable, closed-loop anti-epileptic devices. |
format | Online Article Text |
id | pubmed-8341467 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
record_format | MEDLINE/PubMed |
spelling | pubmed-83414672021-08-05 Model-based design for seizure control by stimulation Ashourvan, Arian Pequito, Sérgio Khambhati, Ankit N Mikhail, Fadi Baldassano, Steven N Davis, Kathryn A Lucas, Timothy H Vettel, Jean M Litt, Brian Pappas, George J Bassett, Danielle S J Neural Eng Article OBJECTIVE. Current brain stimulation paradigms are largely empirical rather than theoretical. An opportunity exists to improve upon their modest effectiveness in closed-loop control strategies with the development of theoretically grounded, model-based designs. APPROACH. Inspired by this need, here we couple experimental data and mathematical modeling with a control-theoretic strategy for seizure termination. We begin by exercising a dynamical systems approach to model seizures (n = 94) recorded using intracranial EEG (iEEG) from 21 patients with medication-resistant, localization-related epilepsy. MAIN RESULTS. Although each patient’s seizures displayed unique spatial and temporal patterns, their evolution can be parsimoniously characterized by the same model form. Idiosyncracies of the model can inform individualized intervention strategies, specifically in iEEG samples with well-localized seizure onset zones. Temporal fluctuations in the spatial profiles of the oscillatory modes show that seizure onset marks a transition into a regime in which the underlying system supports prolonged rhythmic and focal activity. Based on these observations, we propose a control-theoretic strategy that aims to stabilize ictal activity using static output feedback for linear time-invariant switching systems. Finally, we demonstrate in silico that our proposed strategy allows us to dampen the emerging focal oscillatory sources using only a small set of electrodes. SIGNIFICANCE. Our integrative study informs the development of modulation and control algorithms for neurostimulation that could improve the effectiveness of implantable, closed-loop anti-epileptic devices. 2020-03-26 /pmc/articles/PMC8341467/ /pubmed/32103826 http://dx.doi.org/10.1088/1741-2552/ab7a4e Text en https://creativecommons.org/licenses/by/4.0/Original content from this work may be used under the terms of the Creative Commons Attribution 4.0 licence. |
spellingShingle | Article Ashourvan, Arian Pequito, Sérgio Khambhati, Ankit N Mikhail, Fadi Baldassano, Steven N Davis, Kathryn A Lucas, Timothy H Vettel, Jean M Litt, Brian Pappas, George J Bassett, Danielle S Model-based design for seizure control by stimulation |
title | Model-based design for seizure control by stimulation |
title_full | Model-based design for seizure control by stimulation |
title_fullStr | Model-based design for seizure control by stimulation |
title_full_unstemmed | Model-based design for seizure control by stimulation |
title_short | Model-based design for seizure control by stimulation |
title_sort | model-based design for seizure control by stimulation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8341467/ https://www.ncbi.nlm.nih.gov/pubmed/32103826 http://dx.doi.org/10.1088/1741-2552/ab7a4e |
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